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Project Revoice
Project Revoice is a initiative with the ultimate goal to ensure that no one living with ALS will ever have to suffer being robbed of their voice.
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National ALS Registry
The National ALS Registry is a congressionally mandated registry for persons in the U.S. with ALS. It is the only population-based registry in the U.S. that collects information to help scientists learn more about who gets ALS and its causes.
Learn MoreWhether you’re newly diagnosed, navigating your journey with the disease, caring for a person with ALS, or researching the cure, there are resources to support you.
Let us help you and your family cope with the day-to-day challenges of living with ALS.
For People with ALS
Learn about our grant program, upcoming scientific meetings, and opportunities to collaborate.
For Researchers
Caring for someone with ALS is hard work. We offer resources and support to help you.
For Caregivers- Fran McClellan Awarded the Lawrence A. Rand Prize
January 11, 2019 - Terry Bradshaw Teams Up with The ALS Association to Raise Awareness of ALS
January 8, 2019 - Collaboration and Hope in Glasgow: A Look Back at the Annual ALS/MND Meetings and Research Symposium
January 7, 2019 - Guest Post: ‘Give ALS Researchers Hope’
December 28, 2018
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Your gift will help The ALS Association support research to find a cure for ALS and provide much-needed services to patients and their families. By becoming a part of The ALS Association family and making your gift today, you will help sustain hope in thousands of people affected by ALS.